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Year Number of Results
1991 1
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1999 2
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2003 4
2004 1
2006 6
2007 3
2008 5
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2010 5
2011 5
2012 4
2013 6
2014 6
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Page 1
Editorial.
Psillakis E, Pichon V. Psillakis E, et al. Among authors: pichon v. J Sep Sci. 2022 Jan;45(1):6. doi: 10.1002/jssc.202270014. J Sep Sci. 2022. PMID: 34981896 No abstract available.
Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation.
Mourozeau L, Pichon V, Bouzidi A, Charif M, Tessarech M, Caignard A, Amati-Bonneau P, Guichet A, Lavigne C, Verny C, Gohier P, Lenaers G. Mourozeau L, et al. Among authors: pichon v. Ocul Immunol Inflamm. 2025 Jul;33(5):849-853. doi: 10.1080/09273948.2025.2453873. Epub 2025 Jan 23. Ocul Immunol Inflamm. 2025. PMID: 39847428
French guidelines for the diagnosis and management of pure hereditary spastic paraplegia.
Mania-Pâris L, Ewenczyk C, Nicolas G, Anheim M, Durr A, Pichon B, Isner-Horobeti ME, Angelini C, Goizet C, Roubertie A, Soudrie B, Davion JB, Marolleau I, Maumy I, Pichon V, Thauvin C, Thomas Q. Mania-Pâris L, et al. Among authors: pichon v. Rev Neurol (Paris). 2025 Jun;181(6):471-482. doi: 10.1016/j.neurol.2025.05.001. Epub 2025 May 30. Rev Neurol (Paris). 2025. PMID: 40450402 Free article.
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.
Harrer P, Krygier M, Krenn M, Kittke V, Danis M, Krastev G, Saparov A, Pichon V, Malbos M, Scherer C, Dzinovic I, Skorvanek M, Kopajtich R, Prokisch H, Silvaieh S, Grisold A, Mazurkiewicz-Bełdzińska M, de Sainte Agathe JM, Winkelmann J, Necpal J, Jech R, Zech M. Harrer P, et al. Among authors: pichon v. Mov Disord. 2025 Jul;40(7):1388-1400. doi: 10.1002/mds.30209. Epub 2025 Apr 25. Mov Disord. 2025. PMID: 40276935 Free PMC article.
115 results